Canonical Allele Identifier: CA372255352
Gene: NDRG1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.133250478G>C , CM000670.2:g.133250478G>C GRCh38
NC_000008.10:g.134262721G>C , CM000670.1:g.134262721G>C GRCh37
NC_000008.9:g.134331903G>C NCBI36
NG_007943.1:g.51778C>G , LRG_258:g.51778C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000323851.13:c.660C>G MANE Select ENSP00000319977.8:p.Asn220Lys
ENST00000537882.3:c.660C>G ENSP00000437443.2:p.Asn220Lys
ENST00000675172.1:c.256C>G ENSP00000502297.1:n.256C>G
ENST00000675273.1:n.58-1707C>G
ENST00000675860.1:n.425C>G
ENST00000676142.1:n.66C>G
ENST00000676444.1:n.691C>G
ENST00000323851.11:c.660C>G ENSP00000319977.7:p.Asn220Lys
ENST00000414097.6:c.660C>G ENSP00000404854.2:p.Asn220Lys
ENST00000517331.5:n.378C>G
ENST00000517599.5:c.*266C>G ENSP00000429172.1:n.*266C>G
ENST00000518066.5:c.37-8422C>G ENSP00000431057.1:n.37-8422C>G
ENST00000518176.5:c.49-3815C>G ENSP00000429007.1:n.49-3815C>G
ENST00000519278.5:n.1756C>G
ENST00000521664.1:n.410C>G
ENST00000522377.5:c.*140C>G ENSP00000429380.1:n.*140C>G
ENST00000522476.5:c.462C>G ENSP00000427894.1:p.Asn154Lys
ENST00000537882.2:c.417C>G ENSP00000437443.1:p.Asn139Lys
NM_001135242.1:c.660C>G NP_001128714.1:p.Asn220Lys
NM_001258432.1:c.462C>G NP_001245361.1:p.Asn154Lys
NM_001258433.1:c.417C>G NP_001245362.1:p.Asn139Lys
NM_006096.3:c.660C>G , LRG_258t1:c.660C>G NP_006087.2:p.Asn220Lys
XM_011516791.1:c.711C>G XP_011515093.1:p.Asn237Lys
XM_011516792.1:c.93C>G XP_011515094.1:p.Asn31Lys
XM_011516792.2:c.93C>G XP_011515094.1:p.Asn31Lys
NM_001135242.2:c.660C>G NP_001128714.1:p.Asn220Lys
NM_001258432.2:c.462C>G NP_001245361.1:p.Asn154Lys
NM_001258433.2:c.417C>G NP_001245362.1:p.Asn139Lys
NM_001374844.1:c.711C>G NP_001361773.1:p.Asn237Lys
NM_001374845.1:c.660C>G NP_001361774.1:p.Asn220Lys
NM_001374846.1:c.660C>G NP_001361775.1:p.Asn220Lys
NM_001374847.1:c.462C>G NP_001361776.1:p.Asn154Lys
NM_006096.4:c.660C>G MANE Select NP_006087.2:p.Asn220Lys